Literature DB >> 31847782

Investigation of conformational dynamics of Tyr89Cys mutation in protection of telomeres 1 gene associated with familial melanoma.

Mohd Amir1, Shahzaib Ahamad2, Taj Mohammad1, Deeba Shamim Jairajpuri3, Gulam Mustafa Hasan4, Ravins Dohare1, Asimul Islam1, Faizan Ahmad1, Md Imtaiyaz Hassan1.   

Abstract

Protection of telomeres 1 (POT1) is a component of the shelterin complex which is crucial for the regulation of telomere length and maintenance. Many naturally occurring mutations in the POT1 gene have been found to be associated with cardiac angiosarcoma, glioma, familial melanoma, and chronic lymphocytic leukemia. In particular, Y89C is a naturally occurring mutation of POT1, responsible for familial melanoma, and the molecular basis of this mutation is unexplored. In this study, we have extensively analyzed the structure of WT and Y89C mutant of POT1 to see the change in the conformational dynamics, free energy landscape, molecular motions and configurational frustration using molecular dynamics (MD) and other bioinformatics approaches. Y89C mutation shows a significant change in the backbone orientation, compactness, residual fluctuation, solvent accessibility, and hydrogen bonding, suggesting an overall destabilization of the protein structure. Besides, essential dynamics, conformation, magnitude, direction of motion and frustration analysis further suggesting the structural loss in POT1 due to Y89C mutation. Free energy landscape analysis also indicates the presence of a single well-defined free-energy minima in case of WT compared to multiple wells defined free energy minima observed in Y89C, clearly suggesting that this mutation leads to reduce the stability of POT1. This study possibly provides a valuable path to understand the molecular basis of Y89C-mediated development of familial melanoma.Communicated by Ramaswamy H. Sarma.

Entities:  

Keywords:  FEL analysis; OB folds protein; molecular dynamics simulation; mutational landscape analysis; protection of telomere 1; shelterin complex

Mesh:

Substances:

Year:  2019        PMID: 31847782     DOI: 10.1080/07391102.2019.1705186

Source DB:  PubMed          Journal:  J Biomol Struct Dyn        ISSN: 0739-1102


  4 in total

1.  Frustration analysis of TBK1 missense mutations reported in ALS/FTD and cancer patients.

Authors:  Fatima Khatoon; Vijay Kumar; Farah Anjum; Alaa Shafie; Mohd Adnan; Md Imtaiyaz Hassan
Journal:  3 Biotech       Date:  2022-07-14       Impact factor: 2.893

2.  Investigating single amino acid substitutions in PIM1 kinase: A structural genomics approach.

Authors:  Alaa Shafie; Shama Khan; Sagar Batra; Farah Anjum; Taj Mohammad; Shoaib Alam; Dharmendra Kumar Yadav; Asimul Islam; Md Imtaiyaz Hassan
Journal:  PLoS One       Date:  2021-10-22       Impact factor: 3.240

3.  Impact of Single Amino Acid Substitutions in Parkinsonism-Associated Deglycase-PARK7 and Their Association with Parkinson's Disease.

Authors:  Farah Anjum; Namrata Joshia; Taj Mohammad; Alaa Shafie; Fahad A Alhumaydhi; Mohammad A Aljasir; Moyad J S Shahwan; Bekhzod Abdullaev; Mohd Adnan; Abdelbaset Mohamed Elasbali; Visweswara Rao Pasupuleti; Md Imtaiyaz Hassan
Journal:  J Pers Med       Date:  2022-02-05

Review 4.  Structural Features of Nucleoprotein CST/Shelterin Complex Involved in the Telomere Maintenance and Its Association with Disease Mutations.

Authors:  Mohd Amir; Parvez Khan; Aarfa Queen; Ravins Dohare; Mohamed F Alajmi; Afzal Hussain; Asimul Islam; Faizan Ahmad; Imtaiyaz Hassan
Journal:  Cells       Date:  2020-02-04       Impact factor: 7.666

  4 in total

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